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Cardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutantHENDERSON, Deborah J; CONWAY, Simon J; GREENE, Nicholas D. E et al.Circulation research. 2001, Vol 89, Num 1, pp 6-12, issn 0009-7330Article

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityPAGNAMENTA, Alistair T; KHAN, Hameed; PINTO, Dalila et al.Journal of medical genetics. 2011, Vol 48, Num 1, pp 48-54, issn 0022-2593, 7 p.Article

Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox GeneTWIGG, Stephen R. F; VERSNEL, Sarah L; ROBINSON, Alexis A et al.American journal of human genetics. 2009, Vol 84, Num 5, pp 698-705, issn 0002-9297, 8 p.Article

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